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FDA 510(k)

BD MiniDraw Capillary Blood Collection System with BD MiniDraw H&H Capillary Blood Collection Tube

K-Number: K230493 · 2023-11-27

Decision Date2023-11-27
Product CodeGIM
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

BD MiniDraw Capillary Blood Collection System with BD MiniDraw H&H Capillary Blood Collection Tube is a medical device manufactured by Becton, Dickinson and Company. It received FDA 510(k) clearance on 2023-11-27 under approval number K230493. The device is classified under product code GIM. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BD MiniDraw Capillary Blood Collection System with BD MiniDraw H&H Capillary Blood Collection Tube?

BD MiniDraw Capillary Blood Collection System with BD MiniDraw H&H Capillary Blood Collection Tube is a medical device that received FDA 510(k) clearance on 2023-11-27. It is manufactured by Becton, Dickinson and Company. The 510(k) number is K230493.

When was BD MiniDraw Capillary Blood Collection System with BD MiniDraw H&H Capillary Blood Collection Tube approved by the FDA?

BD MiniDraw Capillary Blood Collection System with BD MiniDraw H&H Capillary Blood Collection Tube received FDA 510(k) clearance on 2023-11-27, under approval number K230493.

What company makes BD MiniDraw Capillary Blood Collection System with BD MiniDraw H&H Capillary Blood Collection Tube?

BD MiniDraw Capillary Blood Collection System with BD MiniDraw H&H Capillary Blood Collection Tube is manufactured by Becton, Dickinson and Company.

What is the FDA product code for BD MiniDraw Capillary Blood Collection System with BD MiniDraw H&H Capillary Blood Collection Tube?

The FDA product code for BD MiniDraw Capillary Blood Collection System with BD MiniDraw H&H Capillary Blood Collection Tube is GIM.

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Official Source

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